Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs10144436
DICER1
1.000 0.040 14 95090065 3 prime UTR variant C/A snv 2.9E-02 1
rs10170218 1.000 0.040 2 187949717 intron variant A/C snv 0.25 1
rs1033962
PRTFDC1
1.000 0.040 10 24927877 intron variant C/T snv 0.33 1
rs1042357
ALOX12 ; ALOX12-AS1
0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10744891
NOS1
1.000 0.040 12 117284536 intron variant G/T snv 0.41 1
rs10852889
ALOX12 ; ALOX12-AS1
1.000 0.040 17 6997526 intron variant C/A;G;T snv 1
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs11599164
ANK3
1.000 0.040 10 60072226 missense variant G/T snv 7.2E-02 7.3E-02 1
rs1187327
NTRK2
1.000 0.040 9 84673625 intron variant T/C snv 0.50 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs12364283
DRD2 ; LOC105369501
0.925 0.080 11 113476233 upstream gene variant A/G snv 5.8E-02 3
rs12458282
MBP
1.000 0.040 18 77061897 intron variant T/C snv 0.24 1
rs12898919
CHRNA5
1.000 0.040 15 78588235 intron variant G/C snv 3.1E-02 1
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs12944712
CRHR1 ; LINC02210-CRHR1
0.925 0.040 17 45793781 intron variant G/A snv 0.35 3
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1374141592
FLT4
1.000 0.040 5 180630561 missense variant C/T snv 7.0E-06 1
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs159572
ANKRD55
1.000 0.040 5 56211219 intron variant A/C snv 0.37 1
rs16904179
CYRIB
1.000 0.040 8 129946705 intron variant G/A snv 6.2E-02 1